Sodium Hydroxide → HCID 20061667, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][C:14]2[N:15]([CH3:25])[C:16]([CH2:19][C:20]([O:22]CC)=[O:21])=[CH:17][CH:18]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[OH-].[Na+]>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][CH2:12][CH2:13][C:14]2[N:15]([CH3:25])[C:16]([CH2:19][C:20]([OH:22])=[O:21])=[CH:17][CH:18]=2)(=[O:9])=[O:10])=[CH:4][CH:3]=1Participants
3
Procedure
0.5 g (1.3 mmol) of ethyl [2-(2-(4-fluorobenzenesulphonylamino)-ethyl)-1-methylpyrrol-5-yl]acetate are stirred into 4.5 ml of 1N of sodium hydroxide solution overnight at ambient temperature. The mixture is then extracted with ethylene chloride and the aqueous phase is acidified with 1N hydrochloric acid. The precipitate obtained is suction filtered and dried.
Workup
- extractionThe mixture is then extracted with ethylene chloride
- customThe precipitate obtained
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-72c116df245a44038d25934c85cd46f7
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870076
Reaction notes
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